| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154486557-154486760 | Rare:29 | ||||
| chrX:154490614-154490791 | Common:2; Rare:45 | ||||
| chrX:154516114-154516536 | Common:4; Rare:83 | ||||
| chrX:154533115-154533390 | Common:2; Rare:47; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chrX:154541053-154541302 | Rare:39 | ||||
| chrX:154542030-154542303 | Rare:52; Clinvar:1 | ||||
| chrX:154546034-154546341 | Rare:56; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chrX:154546772-154547020 | Common:1; Rare:86 | ||||
| chrX:154547221-154547473 | Rare:47 | ||||
| chrX:154547533-154547714 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chrX:154762615-154762981 | Common:4; Rare:80; Clinvar:2 | ||||
| chrX:154805360-154805583 | Rare:42 | ||||
| chrX:155026751-155027059 | Rare:84 | ||||
| chrX:155070946-155071542 | Common:2; Rare:119 | ||||
| chrX:155216279-155216513 | Rare:43 |